GMP as per ICH guidelines Good Manufacturing Practices .
GMP = "Good manufacturing practice".GMP is a set of practices and systems that have to be used in pharmaceutical industry (manufacturing, quality control, testing). These are general principles, not not prescriptive instructions.In United States GMP is enforced by the FDA.
Paul L. Simmons has written: 'The impact of GMP's in pharmaceutical and nutraceutical manufacturing' 'The impact of GMP's on the manufacture of bulk pharmaceutical chemicals/biologics' -- subject(s): Pharmaceutical technology, Quality control, Standards 'The design, construction and commissioning of a new facility in accordance with GMP regulations'
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Association of the British Pharmaceutical Industry was created in 1891.
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Carol DeSain has written: 'Documentation basics that support good manufacturing practices' -- subject(s): Documentation, Quality control, Pharmaceutical industry, Manufactures 'Documentation Basics That Support Good Manufacturing Practices and Quality System Regulations' 'Implementing international drug, device, and diagnostic GMP's' -- subject(s): Standards, Quality control, Pharmaceutical industry, Drugs, Medical instruments and apparatus industry, Medical instruments and apparatus, Diagnostic equipment industry, Equipment and supplies, Diagnosis
The production department in the pharmaceutical industry is responsible for manufacturing pharmaceutical products. These products include pills and other medical agents.
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MS In Pharmaceutical Chemistry.